Human genes for mal de Meleda
Mal de Meleda [DOID:0060862]
A palmoplantar keratosis characterized by autosomal recessive inheritance of symmetric palmoplantar hyperkeratosis that progressively extends to the dorsal surfaces of hands and feet and ichthyotic changes elsewhere that has material_basis_in homozygous mutation in the SLURP1 gene on chromosome 8q24.
Synonyms: mal de Meleda, DOID:0060862, mal de Meledas, keratosis palmoplantaris transgrediens of Siemens, Meleda disease ...